Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype

Rationale: The relationship between clinical phenotype of childhood primary ciliary dyskinesia (PCD) and ultrastructural defects and genotype is poorly defined. Objectives: To delineate clinical features of childhood PCD and their associations with ultrastructural defects and genotype. Methods: A to...

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Vydáno v:Am J Respir Crit Care Med
Hlavní autoři: Davis, Stephanie D., Ferkol, Thomas W., Rosenfeld, Margaret, Lee, Hye-Seung, Dell, Sharon D., Sagel, Scott D., Milla, Carlos, Zariwala, Maimoona A., Pittman, Jessica E., Shapiro, Adam J., Carson, Johnny L., Krischer, Jeffrey P., Hazucha, Milan J., Cooper, Matthew L., Knowles, Michael R., Leigh, Margaret W.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Thoracic Society 2015
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Original Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4351577/
https://ncbi.nlm.nih.gov/pubmed/25493340
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1164/rccm.201409-1672OC
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